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Melicope borbonica

Table of Contents

Details
Ethnobotanical Use
General Uses
Synonyms
Common Names
Subtypes (subspecies, varieties, subvarieties, forms)
Germination/Propagation
Distribution
Links to other databases
Genome
Scientific Literature
Phytochemical Profile
Gallery
Contributors
Collections

Details Top

Internal ID UUID643ffe77f1d75396688717
Scientific name Melicope borbonica
Authority (Bory) T.G.Hartley
First published in Allertonia 8: 287 (2001)

Ethnobotanical Use Top

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General Uses Top

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Synonyms Top

Scientific name Authority First published in
Aubertia borbonica Bory Voy. îles Afrique 1: 356 (1804)
Evodia aubertia Cordem. Fl. Réunion 367 1895
Evodia borbonica (Bory) Engl. Nat. Pflanzenfam. 3(4): 119 1896
Zanthoxylum aubertia DC. Prodr. [A. P. de Candolle] 1: 725. 1824 [mid Jan 1824]
Euodia aubertia Benth. & Hook.f. ex B.D.Jacks. Index Kew. 1: 939 (1893)
Euodia borbonica (Bory) Engl. Nat. Pflanzenfam. 3(4): 119 (1896)

Common names Top

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Subspecies (abbr. subsp./ssp.) Top

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Varieties (abbr. var.) Top

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Name Authority First published in
Melicope borbonica var. acuminata (Coode) T.G.Hartley Allertonia 8: 287 (2001)
Melicope borbonica var. borbonica Unknown

Subvarieties (abbr. subvar.) Top

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Forms (abbr. f.) Top

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Germination/Propagation Top

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Distribution (via POWO/KEW) Top

Legend for the distribution data:
- Doubtful data
- Extinct
- Introduced
- Native

Links to other databases Top

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Database ID/link to page
World Flora Online wfo-0000453374
Tropicos 100402142
INPN 706523
KEW urn:lsid:ipni.org:names:1020023-1
Open Tree Of Life 5747666
NCBI Taxonomy 1487095
IPNI 1020023-1
iNaturalist 1236696
GBIF 7269132
EPPO MLQBO
Elurikkus 580789

Genomes (via NCBI) Top

No reference genome is available on NCBI yet. We are constantly monitoring for new data.

Scientific Literature Top

Below are displayed the latest 15 articles published in PMC (PubMed Central®) and other sources (DOI number only)!
If you wish to see all the related articles click here.
Title Authors Publication Released IDs
Natural-derived acetophenones: chemistry and pharmacological activities Ahmadpourmir H, Attar H, Asili J, Soheili V, Taghizadeh SF, Shakeri A Nat Prod Bioprospect 10-May-2024
PMCID:PMC11087454
doi:10.1007/s13659-024-00447-x
PMID:38727781
Do Native and Alien Species Differ in Their Ecological Strategies? A Test with Woody Plants in Tropical Rainforests on Réunion Island (Mascarene Archipelago, Indian Ocean) Heymans L, Meyer JY, Ah-Peng C, Ethève Q, Flores O, Lavergne C, Mallet B, Parlevliet H, Strasberg D, Pouteau R Plants (Basel) 27-Nov-2023
PMCID:PMC10708162
doi:10.3390/plants12233990
PMID:38068626
Antifungal Resistance, Metabolic Routes as Drug Targets, and New Antifungal Agents: An Overview about Endemic Dimorphic Fungi Parente-Rocha JA, Bailão AM, Amaral AC, Taborda CP, Paccez JD, Borges CL, Pereira M Mediators Inflamm 13-Jun-2017
PMCID:PMC5485324
doi:10.1155/2017/9870679
PMID:28694566
Screening for biological activity and chemical composition of Euodia borbonica var. borbonica (Rutaceae), a medicinal plant in Reunion Island. Valenciennes E, Smadja J, Conan JY J Ethnopharmacol 01-Mar-1999
doi:10.1016/S0378-8741(98)00137-8
PMID:10363846

Phytochemical Profile Top

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Below are displayed the proven (via scientific papers) natural compounds!
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Name PubChem ID Canonical SMILES MW Found in Proof
> Organic oxygen compounds / Organooxygen compounds / Carbonyl compounds / Phenylketones / Alkyl-phenylketones
Xanthoxylin 66654 Click to see 196.20 unknown https://doi.org/10.1016/S0378-8741(98)00137-8
> Phenylpropanoids and polyketides / Coumarins and derivatives
5,7-Dimethoxycoumarin 2775 Click to see 206.19 unknown https://doi.org/10.1016/S0378-8741(98)00137-8
Scoparone 8417 Click to see 206.19 unknown https://doi.org/10.1016/S0378-8741(98)00137-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens
Psoralen 6199 Click to see 186.16 unknown https://doi.org/10.1016/S0378-8741(98)00137-8
> Phenylpropanoids and polyketides / Coumarins and derivatives / Furanocoumarins / Psoralens / 5-methoxypsoralens
Bergapten 2355 Click to see COC1=C2C=CC(=O)OC2=CC3=C1C=CO3 216.19 unknown https://doi.org/10.1016/S0378-8741(98)00137-8

Gallery Top

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Collections Top

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